Department of Oncology, General Hospital of Western Theatre Command, No. 270, Tianhui Road, Rongdu Avenue, Jinniu District, Chengdu, 610000, Sichuan, People's Republic of China.
Department of Pathology, General Hospital of Western Theatre Command, Chengdu, Sichuan, People's Republic of China.
BMC Urol. 2022 Aug 9;22(1):123. doi: 10.1186/s12894-022-01075-8.
Adenocarcinoma of the rete testis (AORT) is an extremely rare malignant tumor with poor prognosis and limited responsiveness to traditional chemotherapy. Few previous studies have focused on the molecular mechanisms underlying therapy resistance in AORT and further scrutiny is required to enable searches for targeted drugs to guide treatment selection.
The current case concerns a 55-year-old man with AORT who presented with isolated bone metastasis at initial diagnosis and experienced rapid disease progression after multi-line platinum-based combination chemotherapy. Next-generation sequencing revealed a novel somatic lysine methyltransferase 2C (KMT2C) c.5605 T > C mutation in exon 36 with an abundance of 49.27%. The patient received antiangiogenic drug treatment for 2 months but this was discontinued due to unacceptable anorexia and nausea. He survived for 12 months after diagnosis.
A potential correlation between AORT primary multi-drug resistance and KMT2C mutations is implied. Further studies are needed to determine the efficacy of PARP1/2 inhibitors for tumors with KMT2C mutations.
睾丸网腺癌(AORT)是一种极其罕见的恶性肿瘤,预后差,对传统化疗反应有限。以前的研究很少关注 AORT 治疗耐药的分子机制,需要进一步研究以寻找靶向药物来指导治疗选择。
本病例为一名 55 岁男性,初诊时表现为孤立性骨转移,在接受多线铂类联合化疗后疾病迅速进展。下一代测序显示第 36 外显子中存在新型赖氨酸甲基转移酶 2C(KMT2C)c.5605T>C 突变,丰度为 49.27%。患者接受了抗血管生成药物治疗 2 个月,但由于无法耐受厌食和恶心而停止治疗。患者从诊断到死亡共存活了 12 个月。
AORT 原发性多药耐药与 KMT2C 突变之间可能存在相关性。需要进一步研究来确定 PARP1/2 抑制剂对 KMT2C 突变肿瘤的疗效。